DHD(IB)CMPO
carbamylalkylphosphine oxide
C22H46NO2P not CHON
387.589 g/mol
Factor | Value | Conc. | Add. ligand | Aq. acid | Organic diluent | Temp. | Contact time | Additional | Ref. |
---|---|---|---|---|---|---|---|---|---|
Am(III)/Fe(III) | 0.45 | 0.5 M | HNO3 0.01 M | p-diisopropylbenzene | 25°C | 1 min | [1] | ||
Am(III)/Fe(III) | 23 | 0.5 M | HNO3 0.10 M | p-diisopropylbenzene | 25°C | 1 min | [1] | ||
Am(III)/Fe(III) | 24 | 0.5 M | HNO3 0.25 M | p-diisopropylbenzene | 25°C | 1 min | [1] | ||
Am(III)/Fe(III) | 23 | 0.5 M | HNO3 0.50 M | p-diisopropylbenzene | 25°C | 1 min | [1] | ||
Am(III)/Fe(III) | 14 | 0.5 M | HNO3 1.00 M | p-diisopropylbenzene | 25°C | 1 min | [1] | ||
Am(III)/Fe(III) | 3.8 | 0.5 M | HNO3 2.00 M | p-diisopropylbenzene | 25°C | 1 min | [1] | ||
Am(III)/Fe(III) | 0.41 | 0.5 M | HNO3 4.00 M | p-diisopropylbenzene | 25°C | 1 min | [1] | ||
Am(III)/Fe(III) | 0.046 | 0.5 M | HNO3 6.00 M | p-diisopropylbenzene | 25°C | 1 min | [1] | ||
Am/Fe | 6.1 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am/Y | 1.4 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am/Zr | 0.02 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am/Mo | 0.12 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am/Tc | 3.9 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am/Ru | 69 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am/Rh | 92 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am/Pd | 2.4 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am/La | 3.8 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am/Ce | 1.6 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am/Pr | 1.2 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am/Nd | 1.1 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am/Sm | 0.79 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am/Eu | 0.79 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] |
Element | Value | Conc. | Add. ligand | Aq. acid | Organic diluent | Temp. | Contact time | Additional | Ref. |
---|---|---|---|---|---|---|---|---|---|
Am(III) | 3.65 | 0.5 M | HNO3 0.01 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Am(III) | 144 | 0.5 M | HNO3 0.10 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Am(III) | 210 | 0.5 M | HNO3 0.25 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Am(III) | 172 | 0.5 M | HNO3 0.50 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Am(III) | 71.4 | 0.5 M | HNO3 1.00 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Am(III) | 19.7 | 0.5 M | HNO3 2.00 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Am(III) | 6.05 | 0.5 M | HNO3 4.00 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Am(III) | 4.34 | 0.5 M | HNO3 6.00 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Fe(III) | 8.05 | 0.5 M | HNO3 0.01 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Fe(III) | 6.36 | 0.5 M | HNO3 0.10 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Fe(III) | 8.72 | 0.5 M | HNO3 0.25 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Fe(III) | 7.44 | 0.5 M | HNO3 0.50 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Fe(III) | 5.21 | 0.5 M | HNO3 1.00 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Fe(III) | 5.25 | 0.5 M | HNO3 2.00 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Fe(III) | 14.7 | 0.5 M | HNO3 4.00 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Fe(III) | 93.4 | 0.5 M | HNO3 6.00 M | p-diisopropylbenzene | 25°C | 1 min | [2] | ||
Fe | 0.18 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Y | 0.79 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Zr | 55 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Mo | 9.2 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Tc | 0.28 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Ru | 0.016 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Rh | 0.012 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Pd | 0.46 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
La | 0.29 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Ce | 0.69 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Pr | 0.92 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Nd | 1 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Sm | 1.4 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Eu | 1.4 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am | 1.1 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am | ≈50 | 0.25 M | HNO3 0.25 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am | ≈48 | 0.25 M | HNO3 0.5 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am | ≈23 | 0.25 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am | ≈1.2 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [2] | ||
Am | ≈0.3 | 0.25 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [2] |